NDC 17856-4070 Phenytoin
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 17856 - Atlantic Biologicals Corp.
- 17856-4070 - Phenytoin
Product Characteristics
Product Packages
NDC Code 17856-4070-1
Package Description: 72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE / 4 mL in 1 CUP, UNIT-DOSE (17856-4070-2)
Product Details
What is NDC 17856-4070?
What are the uses for Phenytoin?
Which are Phenytoin UNII Codes?
The UNII codes for the active ingredients in this product are:
- PHENYTOIN (UNII: 6158TKW0C5)
- PHENYTOIN (UNII: 6158TKW0C5) (Active Moiety)
Which are Phenytoin Inactive Ingredients UNII Codes?
The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:
- CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
- MAGNESIUM ALUMINUM SILICATE (UNII: 6M3P64V0NC)
- POLYSORBATE 60 (UNII: CAL22UVI4M)
- WATER (UNII: 059QF0KO0R)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Phenytoin?
- RxCUI: 1313112 - phenytoin 125 MG in 5 mL Oral Suspension
- RxCUI: 1313112 - phenytoin 25 MG/ML Oral Suspension
- RxCUI: 1313112 - DPH 25 MG/ML Oral Suspension
- RxCUI: 1313112 - phenytoin 100 MG per 4 ML Oral Suspension
- RxCUI: 1313112 - phenytoin 125 MG per 5 ML Oral Suspension
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Patient Education
Phenytoin
Phenytoin is used to control certain type of seizures, and to treat and prevent seizures that may begin during or after surgery to the brain or nervous system. Phenytoin is in a class of medications called anticonvulsants. It works by decreasing abnormal electrical activity in the brain.
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[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.
[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.
[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".